@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_head {
  this: np:hasAssertion dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_assertion ;
    np:hasProvenance dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_provenance ;
    np:hasPublicationInfo dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_assertion a np:Assertion .
  dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_provenance a np:Provenance .
  dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_assertion {
  miriam-gene:1071 a ncit:C16612 .
  lld:C0856727 a ncit:C7057 .
  dgn-gda:DGN2e1309cfc28926970e33bcc35cc32c87 sio:SIO_000628 miriam-gene:1071 , lld:C0856727 ;
    a sio:SIO_001121 .
}
dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_provenance {
  dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_assertion dcterms:description "[The present data suggest that CETP gene polymorphism may ba associated with cholesterol gallstone disease, probably in combination with some additional factor that reduces the plasma HDL cholesterol concentration, especially in TaqIB B2B2 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:7616125 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP1315241.RAMYvNI8NBqkdQCuwmUD3CQaMu-nToHVcgwN89_-DFeqA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:42+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}